GB318832A - Process for producing fast tints on artificial silk of regenerated cellulose - Google Patents

Process for producing fast tints on artificial silk of regenerated cellulose

Info

Publication number
GB318832A
GB318832A GB27393/29A GB2739329A GB318832A GB 318832 A GB318832 A GB 318832A GB 27393/29 A GB27393/29 A GB 27393/29A GB 2739329 A GB2739329 A GB 2739329A GB 318832 A GB318832 A GB 318832A
Authority
GB
United Kingdom
Prior art keywords
acid
aminophenol
mols
nitro
compounds
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB27393/29A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF Schweiz AG
Original Assignee
Gesellschaft fuer Chemische Industrie in Basel CIBA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Gesellschaft fuer Chemische Industrie in Basel CIBA filed Critical Gesellschaft fuer Chemische Industrie in Basel CIBA
Publication of GB318832A publication Critical patent/GB318832A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B45/00Complex metal compounds of azo dyes
    • C09B45/02Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
    • C09B45/04Azo compounds in general
    • C09B45/06Chromium compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

318,832. Soc. of Chemical Industry in Basle. Sept. 7, 1928, [Convention date]. Azo dyes and soluble chromium. compounds thereof.-Level dyeings, fast to light, water, and washing, are obtained on regenerated cellulose silks by the use of chromium compounds of dyestuffs containing no cyanuric nucleus obtainable by coupling o-oxydiazo or o-carboxydiazo compounds, containing not more than one sulphonic or one carboxylic group and containing no o-oxycarboxylic grouping, with 2 : 5 : 7-aminonaphtholsulphonic acid or its N-acidyl, N-alkyl, N-aralkyl, or N-aryl derivatives. The use of the chromium compounds of Specifications 295,594 and 296,680 is excluded. Dyeing is effected in a neutral' or feebly alkaline bath or in a bath feebly acid with acetic acid. A table is given showing the tints obtained on viscose with the chromium compounds of the following dyestuffs, all couplings being in alkaline solution :-5-nitro-2-aminophenol # phenyl-2 : 5 : 7-acid or (4<1>-oxy-3<1>=carboxy)- phenyl-2 : 5 : 7-acid : 6-nitro-2-aminophenol-4-sulphonic acid, 4 : 6-nitro-2-aminophenol, or anthranilic acid # phenyl-2 : 5 : 7-acid; 4-chloro- 2-aminophenol (2 mols.), 4 (or 5)-nitro-2-aminophenol (2 mols.), 4: 6-dinitro-2-aminophenol (2 mols.), 2-aminophenol-4-sulphamide (2 mols.), or 4-nitro-2-aminophenol-6-sulphonic acid (2 mols.) #2: 2<1>-dinaphthylamine - 5 : 5<1>-dioxy-7 : 7'-disulphonic acid; 5-nitro-2-aminophenol (2 mols.) # the product obtained by coupling tetrazotized benzidine (1 mol.) with 2 2<1>-dinaphthylamine - 5 : 5<1>-dioxy - 7 : 7<1>- disulphonic acid (2 mols.); 2-aminophenol-4-sulphamide (2 mols.) # the urea of 2 : 5 : 7-acid. Specifications 253.659 and 306.908 also are referred to. The Specification as open to inspection under Sect. 91 (3) (a) comprises also the use of the chromium compound of the dyestuff 4-chloro-2- aminophenol (2 mols.) # the product obtained by coupling diazotized 2 : 5 : 7-acid (1 mol.) in acid solution with 2 : 5 : :7-acid (1 mol.) This. subject-matter does not appear in the Specification as accepted.
GB27393/29A 1928-09-07 1929-09-09 Process for producing fast tints on artificial silk of regenerated cellulose Expired GB318832A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH318832X 1928-09-07

Publications (1)

Publication Number Publication Date
GB318832A true GB318832A (en) 1930-12-09

Family

ID=4497368

Family Applications (1)

Application Number Title Priority Date Filing Date
GB27393/29A Expired GB318832A (en) 1928-09-07 1929-09-09 Process for producing fast tints on artificial silk of regenerated cellulose

Country Status (1)

Country Link
GB (1) GB318832A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE914300C (en) * 1951-04-23 1954-07-01 Geigy Ag J R Process for the production of copperable polyazo dyes

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE914300C (en) * 1951-04-23 1954-07-01 Geigy Ag J R Process for the production of copperable polyazo dyes

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